Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_assertion wasGeneratedBy ECO_0000203 NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_assertion wasDerivedFrom befree-20150227 NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_assertion SIO_000772 23969157 NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_assertion evidence source_evidence_literature NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.
- NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_assertion description "[Mutations in the G-protein-coupled receptor PROKR2 have been identified in patients with idiopathic hypogonadotropic hypogonadism (IHH) and Kallmann syndrome (KS) manifesting with delayed puberty and infertility.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP926835.RAJr6Rb0D5oUY_sjVoCm7nl-bKtLoFemOyfm-lIEQfGQQ130_provenance.